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Cellosaurus UOXFi007-B (CVCL_LE38)

[Text version]

Cell line name UOXFi007-B
Synonyms MK002-6
Accession CVCL_LE38
Resource Identification Initiative To cite this cell line use: UOXFi007-B (RRID:CVCL_LE38)
Comments From: University of Oxford; Oxford; United Kingdom.
Omics: Genome sequenced.
Derived from sampling site: Skin; dermis. Cell type=Fibroblast.
Sequence variations
  • Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (EBiSC).
Disease Parkinson's disease (NCIt: C26845)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A8Y3 (MK002)
Sex of cell Female
Age at sampling 72Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections EBiSC; UOXFi007-B - Discontinued
ECACC; 66540549
Cell line databases/resources hPSCreg; UOXFi007-B
Biological sample resources BioSamples; SAMEA103887562
Encyclopedic resources Wikidata; Q54991455
Entry history
Entry creation22-Aug-2017
Last entry update17-Mar-2022
Version number10